Prostaglandin E2

CAS : 363-24-6

Ref. TR-P838610

Informations sur le produit

• Nom: Prostaglandin E2
• Synonymes: Dinoprostone, (Z)-7-[(1R,2R,3R)-3-hydroxy-2-[(E)-(3S)-3-hydroxyoct-1-enyl]-5-oxocyclopentyl]hept-5-enoic acid, PGE2, 5-Heptenoic acid, 7-[3-hydroxy-2-(3-hydroxy-1-octenyl)-5-oxocyclopentyl]- (8CI), 5-Heptenoic acid, 7-[3α-hydroxy-2-(3-hydroxy-1-octenyl)-5-oxocyclopentyl]- (7CI), (5Z,11α,13E,15S)-11,15-Dihydroxy-9-oxoprosta-5,13-dien-1-oic acid, (15S)-Prostaglandin E2, 11,15-Dihydroxy-9-oxoprosta-5,13-dien-1-oic acid (5Z,11α,13E,15S), 11α,15α-Dihydroxy-9-ketoprosta-5,13-dienoic acid, 11α,15α-Dihydroxy-9-oxo-5-cis,13-trans-prostadienoic acid, 5: PN: US20150065431 SEQID: 5 claimed sequence, 7-[3-hydroxy-2-(3-hydroxy-1-octenyl)-5-oxo-cyclopentyl]-5-heptenoic acid, Cervidil, Cerviprime, Cerviprost, Dinoprostone, Enzaprost E, Glandin, Minprositin E2, Minprostin E2, NSC 165560, NSC 196514, Prepidil, Primiprost, Propess, Prostarmon E, Prostenon, Prostenone, Prostin, Prostin (prostaglandin), Prostin E2, U 12062, l-PGE2
• Marque: TRC
• Description: Stability Light SensitiveApplications The most common and biologically potent of mammalian prostaglandins. Oxytocic; abortifacient.References Van Dorp, D.A., et al.: Biochem. Biopphys. Acta, 90, 204 (1964), Hamberg, M., et al.: J. Biol. Chem., 246, 6713 (1971),

Propriétés chimiques

• Masse moléculaire: 352.47
• Formule: C₂₀H₃₂O₅
• Couleur/Forme: White To Beige
• InChI: InChI=1S/C20H32O5/c1-2-3-6-9-15(21)12-13-17-16(18(22)14-19(17)23)10-7-4-5-8-11-20(24)25/h4,7,12-13,15-17,19,21,23H,2-3,5-6,8-11,14H2,1H3,(H,24,25)/b7-4-,13-12+/t15-,16+,17+,19+/m0/s1
• Code InChI: InChIKey=XEYBRNLFEZDVAW-ARSRFYASSA-N
• SMILES: CCCCC[C@H](O)/C=C/[C@H]1[C@H](O)CC(=O)[C@@H]1C/C=C\CCCC(=O)O